Roman Iulian C, Coull Graham, Knowlton Nicholas, Doherty-Eagles Tara, Ozturk Ogün, Michielsen Adriana, Carty Hannah, Yefremenkova Olena, Zăhan Marius
Sims IVF Fertility Clinic, Dublin, Republic of Ireland; Department of Life Sciences and Biotechnology, University of Agricultural Sciences and Veterinary Medicine Cluj-Napoca, Cluj-Napoca, Romania.
Sims IVF Fertility Clinic, Dublin, Republic of Ireland.
Reprod Biomed Online. 2025 Jul;51(1):104828. doi: 10.1016/j.rbmo.2025.104828. Epub 2025 Jan 15.
How does the genetic constitution of embryos impact the accuracy and effectiveness of time-lapse ploidy detection?
A retrospective analysis of chromosomal constitution, morphokinetic characteristics and embryo grading was conducted on 1012 embryos, originating from 386 intracytoplasmic sperm injection cycles at a single clinic. Morphokinetic checkpoints of pronuclear fading, cleavage stages and post-cleavage stages - including start of compaction; time to compacted morula; time to start of blastulation; and time to full, expanded and hatching blastocyst - were recorded for all analysed embryos. Morphokinetic profiles of 363 euploid embryos were used as reference to analyse 649 embryos with aneuploidies, according to their level of gain or loss of chromosomal material. Embryo grading was performed using commercially available time-lapse-based algorithmic embryo selection tools.
Embryos with loss of genetic material and embryos with multiple aneuploidies exhibited consistent developmental delays that accumulated and became significant at the time of blastulation. In contrast, embryos with chromosomal gains displayed a morphokinetic profile almost identical to that of euploid embryos. Subset analyses suggested that aneuploidies of large chromosomes tend to have a greater impact on the morphokinetic profile. Time-lapse-based algorithmic or artificial intelligence scoring downgraded blastocysts with loss of chromosomal material or with complex aneuploidies, but discrimination potential was not observed between embryos with gain of chromosomes and euploid embryos.
Embryos with extra chromosomes show similar morphokinetic patterns to euploid embryos, reducing the effectiveness of non-invasive selection tools. However, embryos with monosomies or multiple aneuploidies experience significant delays in reaching blastulation, and generally score lower on time-lapse selection algorithms.
胚胎的基因构成如何影响延时倍性检测的准确性和有效性?
对来自一家诊所386个卵胞浆内单精子注射周期的1012个胚胎进行了染色体构成、形态动力学特征和胚胎分级的回顾性分析。记录了所有分析胚胎的原核消失、卵裂阶段和卵裂后阶段的形态动力学检查点,包括致密化开始时间;致密桑葚胚形成时间;囊胚形成开始时间;以及完全、扩张和孵化囊胚形成时间。根据染色体物质的增减水平,将363个整倍体胚胎的形态动力学特征用作参考,分析649个非整倍体胚胎。使用市售的基于延时的算法胚胎选择工具进行胚胎分级。
遗传物质缺失的胚胎和具有多个非整倍体的胚胎表现出一致的发育延迟,这些延迟会累积并在囊胚形成时变得显著。相比之下,具有染色体增加的胚胎表现出与整倍体胚胎几乎相同的形态动力学特征。亚组分析表明,大染色体的非整倍体对形态动力学特征的影响往往更大。基于延时的算法或人工智能评分会降低染色体物质缺失或具有复杂非整倍体的囊胚等级,但在染色体增加的胚胎和整倍体胚胎之间未观察到鉴别潜力。
具有额外染色体的胚胎表现出与整倍体胚胎相似的形态动力学模式,降低了非侵入性选择工具的有效性。然而,单体或多个非整倍体的胚胎在达到囊胚形成时会经历显著延迟,并且在延时选择算法上的得分通常较低。